JP2014510788A5 - - Google Patents
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- Publication number
- JP2014510788A5 JP2014510788A5 JP2014505231A JP2014505231A JP2014510788A5 JP 2014510788 A5 JP2014510788 A5 JP 2014510788A5 JP 2014505231 A JP2014505231 A JP 2014505231A JP 2014505231 A JP2014505231 A JP 2014505231A JP 2014510788 A5 JP2014510788 A5 JP 2014510788A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- hydrogen
- unsaturated
- ocf
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 125000000217 alkyl group Chemical group 0.000 claims description 240
- 150000001875 compounds Chemical class 0.000 claims description 168
- 229910052739 hydrogen Inorganic materials 0.000 claims description 129
- 239000001257 hydrogen Substances 0.000 claims description 129
- 229920000728 polyester Polymers 0.000 claims description 100
- 150000003839 salts Chemical class 0.000 claims description 82
- 239000011780 sodium chloride Substances 0.000 claims description 82
- 150000002148 esters Chemical class 0.000 claims description 81
- 239000000651 prodrug Substances 0.000 claims description 81
- 229940002612 prodrugs Drugs 0.000 claims description 81
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 69
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 68
- 150000002431 hydrogen Chemical group 0.000 claims description 60
- 229910052757 nitrogen Inorganic materials 0.000 claims description 60
- 229910052760 oxygen Inorganic materials 0.000 claims description 60
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 60
- 239000001301 oxygen Substances 0.000 claims description 60
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 60
- 125000005842 heteroatoms Chemical group 0.000 claims description 59
- 229910052717 sulfur Inorganic materials 0.000 claims description 59
- 239000011593 sulfur Substances 0.000 claims description 59
- 229910052731 fluorine Inorganic materials 0.000 claims description 52
- 229910052801 chlorine Inorganic materials 0.000 claims description 50
- 229910052736 halogen Inorganic materials 0.000 claims description 50
- 150000002367 halogens Chemical class 0.000 claims description 50
- 229910052794 bromium Inorganic materials 0.000 claims description 48
- 229910052740 iodine Inorganic materials 0.000 claims description 48
- 125000001424 substituent group Chemical group 0.000 claims description 45
- 201000009910 diseases by infectious agent Diseases 0.000 claims description 44
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 41
- 125000003118 aryl group Chemical group 0.000 claims description 30
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 30
- 125000000623 heterocyclic group Chemical group 0.000 claims description 26
- 230000000813 microbial Effects 0.000 claims description 26
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 18
- 125000001188 haloalkyl group Chemical group 0.000 claims description 18
- 125000003342 alkenyl group Chemical group 0.000 claims description 16
- 125000000304 alkynyl group Chemical group 0.000 claims description 14
- 229910052799 carbon Inorganic materials 0.000 claims description 14
- 244000005700 microbiome Species 0.000 claims description 14
- 229940045505 Klebsiella pneumoniae Drugs 0.000 claims description 13
- 241000588747 Klebsiella pneumoniae Species 0.000 claims description 13
- 125000004429 atoms Chemical group 0.000 claims description 12
- 241000606125 Bacteroides Species 0.000 claims description 10
- 206010035664 Pneumonia Diseases 0.000 claims description 10
- RJQXTJLFIWVMTO-TYNCELHUSA-N Methicillin Chemical compound COC1=CC=CC(OC)=C1C(=O)N[C@@H]1C(=O)N2[C@@H](C(O)=O)C(C)(C)S[C@@H]21 RJQXTJLFIWVMTO-TYNCELHUSA-N 0.000 claims description 8
- 210000003491 Skin Anatomy 0.000 claims description 8
- 108020004256 beta-Lactamases Proteins 0.000 claims description 8
- 102000006635 beta-Lactamases Human genes 0.000 claims description 8
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 8
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 229960003085 meticillin Drugs 0.000 claims description 8
- 241000194033 Enterococcus Species 0.000 claims description 7
- 229940031000 Streptococcus pneumoniae Drugs 0.000 claims description 7
- 241000193998 Streptococcus pneumoniae Species 0.000 claims description 7
- 241000588724 Escherichia coli Species 0.000 claims description 6
- 229940047650 Haemophilus influenzae Drugs 0.000 claims description 6
- 241000606768 Haemophilus influenzae Species 0.000 claims description 6
- 229940007042 Proteus vulgaris Drugs 0.000 claims description 6
- 241000588767 Proteus vulgaris Species 0.000 claims description 6
- 229960003165 Vancomycin Drugs 0.000 claims description 6
- 108010059993 Vancomycin Proteins 0.000 claims description 6
- 125000003725 azepanyl group Chemical group 0.000 claims description 6
- 125000002393 azetidinyl group Chemical group 0.000 claims description 6
- 108010068385 carbapenemase Proteins 0.000 claims description 6
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 6
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 6
- 125000003566 oxetanyl group Chemical group 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 125000003386 piperidinyl group Chemical group 0.000 claims description 6
- 125000004076 pyridyl group Chemical group 0.000 claims description 6
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 6
- 239000000758 substrate Substances 0.000 claims description 6
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 6
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 claims description 6
- MYPYJXKWCTUITO-LYRMYLQWSA-O vancomycin(1+) Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C2C=C3C=C1OC1=CC=C(C=C1Cl)[C@@H](O)[C@H](C(N[C@@H](CC(N)=O)C(=O)N[C@H]3C(=O)N[C@H]1C(=O)N[C@H](C(N[C@@H](C3=CC(O)=CC(O)=C3C=3C(O)=CC=C1C=3)C([O-])=O)=O)[C@H](O)C1=CC=C(C(=C1)Cl)O2)=O)NC(=O)[C@@H](CC(C)C)[NH2+]C)[C@H]1C[C@](C)([NH3+])[C@H](O)[C@H](C)O1 MYPYJXKWCTUITO-LYRMYLQWSA-O 0.000 claims description 6
- 241000588919 Citrobacter freundii Species 0.000 claims description 5
- 229940037645 Staphylococcus epidermidis Drugs 0.000 claims description 5
- 241000191963 Staphylococcus epidermidis Species 0.000 claims description 5
- 241000588626 Acinetobacter baumannii Species 0.000 claims description 4
- 241000606219 Bacteroides uniformis Species 0.000 claims description 4
- 229940038704 Clostridium perfringens Drugs 0.000 claims description 4
- 241000193468 Clostridium perfringens Species 0.000 claims description 4
- 241000588914 Enterobacter Species 0.000 claims description 4
- 229940023064 Escherichia coli Drugs 0.000 claims description 4
- 241000605909 Fusobacterium Species 0.000 claims description 4
- 208000008745 Healthcare-Associated Pneumonia Diseases 0.000 claims description 4
- 241000588749 Klebsiella oxytoca Species 0.000 claims description 4
- 241000588655 Moraxella catarrhalis Species 0.000 claims description 4
- 229940049954 Penicillin Drugs 0.000 claims description 4
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 claims description 4
- 241000191992 Peptostreptococcus Species 0.000 claims description 4
- 241001135211 Porphyromonas asaccharolytica Species 0.000 claims description 4
- 229940055033 Proteus mirabilis Drugs 0.000 claims description 4
- 241000588770 Proteus mirabilis Species 0.000 claims description 4
- 241000588768 Providencia Species 0.000 claims description 4
- 229940055023 Pseudomonas aeruginosa Drugs 0.000 claims description 4
- 241000589517 Pseudomonas aeruginosa Species 0.000 claims description 4
- 206010057190 Respiratory tract infection Diseases 0.000 claims description 4
- 206010040872 Skin infection Diseases 0.000 claims description 4
- 229940076156 Streptococcus pyogenes Drugs 0.000 claims description 4
- 241000193996 Streptococcus pyogenes Species 0.000 claims description 4
- 230000001154 acute Effects 0.000 claims description 4
- 230000001580 bacterial Effects 0.000 claims description 4
- 229960000626 benzylpenicillin Drugs 0.000 claims description 4
- 125000002837 carbocyclic group Chemical group 0.000 claims description 4
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
- 125000003678 cyclohexadienyl group Chemical group C1(=CC=CCC1)* 0.000 claims description 4
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 claims description 4
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 4
- 125000004925 dihydropyridyl group Chemical group N1(CC=CC=C1)* 0.000 claims description 4
- 125000002541 furyl group Chemical group 0.000 claims description 4
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims description 4
- 125000005942 tetrahydropyridyl group Chemical group 0.000 claims description 4
- 210000001519 tissues Anatomy 0.000 claims description 4
- 241000606124 Bacteroides fragilis Species 0.000 claims description 3
- 241000588923 Citrobacter Species 0.000 claims description 3
- 241001657508 Eggerthella lenta Species 0.000 claims description 3
- 241001465754 Metazoa Species 0.000 claims description 3
- 229940076185 Staphylococcus aureus Drugs 0.000 claims description 3
- 241000191967 Staphylococcus aureus Species 0.000 claims description 3
- 241000194017 Streptococcus Species 0.000 claims description 3
- 241000186561 [Clostridium] clostridioforme Species 0.000 claims description 3
- 230000002265 prevention Effects 0.000 claims description 3
- 241000589291 Acinetobacter Species 0.000 claims description 2
- 206010060968 Arthritis infective Diseases 0.000 claims description 2
- 229940065181 Bacillus anthracis Drugs 0.000 claims description 2
- 241000193738 Bacillus anthracis Species 0.000 claims description 2
- 206010003997 Bacteraemia Diseases 0.000 claims description 2
- 241000606215 Bacteroides vulgatus Species 0.000 claims description 2
- 210000003555 Cloaca Anatomy 0.000 claims description 2
- 206010014665 Endocarditis Diseases 0.000 claims description 2
- 229940092559 Enterobacter aerogenes Drugs 0.000 claims description 2
- 229940119563 Enterobacter cloacae Drugs 0.000 claims description 2
- 241000588697 Enterobacter cloacae Species 0.000 claims description 2
- 241000606766 Haemophilus parainfluenzae Species 0.000 claims description 2
- 241000588748 Klebsiella Species 0.000 claims description 2
- 241000588915 Klebsiella aerogenes Species 0.000 claims description 2
- 241000589248 Legionella Species 0.000 claims description 2
- 208000007764 Legionnaires' Disease Diseases 0.000 claims description 2
- TYZROVQLWOKYKF-ZDUSSCGKSA-N Linezolid Chemical compound O=C1O[C@@H](CNC(=O)C)CN1C(C=C1F)=CC=C1N1CCOCC1 TYZROVQLWOKYKF-ZDUSSCGKSA-N 0.000 claims description 2
- 241000588771 Morganella <proteobacterium> Species 0.000 claims description 2
- 206010031252 Osteomyelitis Diseases 0.000 claims description 2
- 241000606210 Parabacteroides distasonis Species 0.000 claims description 2
- 210000004197 Pelvis Anatomy 0.000 claims description 2
- 206010034668 Peritoneal infection Diseases 0.000 claims description 2
- 206010034674 Peritonitis Diseases 0.000 claims description 2
- 206010035148 Plague Diseases 0.000 claims description 2
- 241000605861 Prevotella Species 0.000 claims description 2
- 241001135215 Prevotella bivia Species 0.000 claims description 2
- 241000588778 Providencia stuartii Species 0.000 claims description 2
- 206010040047 Sepsis Diseases 0.000 claims description 2
- 229940098362 Serratia marcescens Drugs 0.000 claims description 2
- 241000607715 Serratia marcescens Species 0.000 claims description 2
- 206010058028 Shunt infection Diseases 0.000 claims description 2
- 206010041925 Staphylococcal infection Diseases 0.000 claims description 2
- 241000122973 Stenotrophomonas maltophilia Species 0.000 claims description 2
- 229940030998 Streptococcus agalactiae Drugs 0.000 claims description 2
- 241000193985 Streptococcus agalactiae Species 0.000 claims description 2
- 241000194008 Streptococcus anginosus Species 0.000 claims description 2
- 241001291896 Streptococcus constellatus Species 0.000 claims description 2
- 206010045146 Tularaemia Diseases 0.000 claims description 2
- 206010046577 Urinary tract infection Diseases 0.000 claims description 2
- 230000037006 agalactosis Effects 0.000 claims description 2
- 230000001684 chronic Effects 0.000 claims description 2
- 239000003814 drug Substances 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 238000007912 intraperitoneal administration Methods 0.000 claims description 2
- 229960003907 linezolid Drugs 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 201000009906 meningitis Diseases 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims description 2
- 201000008827 tuberculosis Diseases 0.000 claims description 2
- 230000002792 vascular Effects 0.000 claims description 2
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims 6
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 241000894007 species Species 0.000 claims 2
- 241000606123 Bacteroides thetaiotaomicron Species 0.000 claims 1
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims 1
- 229940092534 Citrobacter koseri Drugs 0.000 claims 1
- 241000588917 Citrobacter koseri Species 0.000 claims 1
- 229940032049 Enterococcus faecalis Drugs 0.000 claims 1
- 241000194032 Enterococcus faecalis Species 0.000 claims 1
- 241000186394 Eubacterium Species 0.000 claims 1
- 206010016256 Fatigue Diseases 0.000 claims 1
- 241001169527 Morganella sp. (in: Fungi) Species 0.000 claims 1
- 241000588769 Proteus <enterobacteria> Species 0.000 claims 1
- 241000588777 Providencia rettgeri Species 0.000 claims 1
- 241000191940 Staphylococcus Species 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- -1 t- butyl Chemical group 0.000 claims 1
- 230000003867 tiredness Effects 0.000 claims 1
- 0 *C(*)(C(*)(*)C(*)(*)N)C(*)(*)c(ccc(*)c1C(NC2=N3)=CC2=CN(c2c(*)c(*)c(C(*)(*)NCCCNC(N)=N)c(I)c2*)C3=O)c1O* Chemical compound *C(*)(C(*)(*)C(*)(*)N)C(*)(*)c(ccc(*)c1C(NC2=N3)=CC2=CN(c2c(*)c(*)c(C(*)(*)NCCCNC(N)=N)c(I)c2*)C3=O)c1O* 0.000 description 9
- 241000282412 Homo Species 0.000 description 2
- 241000204031 Mycoplasma Species 0.000 description 2
- 241000193403 Clostridium Species 0.000 description 1
- 229940076266 Morganella morganii Drugs 0.000 description 1
- 241000588772 Morganella morganii Species 0.000 description 1
- 125000005038 alkynylalkyl group Chemical group 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 230000002194 synthesizing Effects 0.000 description 1
- 238000003419 tautomerization reaction Methods 0.000 description 1
- 230000000699 topical Effects 0.000 description 1
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161476138P | 2011-04-15 | 2011-04-15 | |
| US61/476,138 | 2011-04-15 | ||
| US201161535118P | 2011-09-15 | 2011-09-15 | |
| US61/535,118 | 2011-09-15 | ||
| US201261610363P | 2012-03-13 | 2012-03-13 | |
| US61/610,363 | 2012-03-13 | ||
| PCT/US2012/032994 WO2012173689A2 (en) | 2011-04-15 | 2012-04-11 | Antimicrobial compounds and methods of making and using the same |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018068456A Division JP2018115206A (ja) | 2011-04-15 | 2018-03-30 | 抗菌化合物ならびにそれを作製および使用する方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2014510788A JP2014510788A (ja) | 2014-05-01 |
| JP2014510788A5 true JP2014510788A5 (no) | 2015-05-28 |
| JP6317669B2 JP6317669B2 (ja) | 2018-04-25 |
Family
ID=47357660
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014505231A Active JP6317669B2 (ja) | 2011-04-15 | 2012-04-11 | 抗菌化合物ならびにそれを作製および使用する方法 |
| JP2018068456A Pending JP2018115206A (ja) | 2011-04-15 | 2018-03-30 | 抗菌化合物ならびにそれを作製および使用する方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018068456A Pending JP2018115206A (ja) | 2011-04-15 | 2018-03-30 | 抗菌化合物ならびにそれを作製および使用する方法 |
Country Status (20)
| Country | Link |
|---|---|
| US (2) | US9221827B2 (no) |
| EP (2) | EP2697229B1 (no) |
| JP (2) | JP6317669B2 (no) |
| KR (1) | KR20140065378A (no) |
| CN (2) | CN109053695A (no) |
| AR (1) | AR088781A1 (no) |
| AU (3) | AU2012271228B2 (no) |
| BR (1) | BR112013026410A2 (no) |
| CA (1) | CA2833169A1 (no) |
| DK (1) | DK2697229T3 (no) |
| EA (1) | EA201391536A1 (no) |
| ES (1) | ES2665988T3 (no) |
| HU (1) | HUE036755T2 (no) |
| IL (1) | IL228845A0 (no) |
| MX (1) | MX357903B (no) |
| MY (1) | MY173518A (no) |
| PT (1) | PT2697229T (no) |
| SG (2) | SG10201603027QA (no) |
| TW (2) | TW201843154A (no) |
| WO (1) | WO2012173689A2 (no) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2777741A1 (en) | 2009-10-16 | 2011-04-21 | Rib-X Pharmaceuticals, Inc. | Antimicrobial compounds and methods of making and using the same |
| WO2011047319A2 (en) | 2009-10-16 | 2011-04-21 | Rib-X Pharmaceuticals, Inc. | Antimicrobial compounds and methods of making and using the same |
| WO2011047320A2 (en) | 2009-10-16 | 2011-04-21 | Rib-X Pharmaceuticals, Inc. | Antimicrobial compounds and methods of making and using the same |
| PT2697229T (pt) | 2011-04-15 | 2018-04-13 | Melinta Therapeutics Inc | Compostos antimicrobianos e seus métodos de fabrico e de utilização |
| US9718816B2 (en) | 2013-03-15 | 2017-08-01 | Epizyme, Inc. | 1-phenoxy-3-(alkylamino)-propan-2-ol derivatives as CARM1 inhibitors and uses thereof |
| US9346802B2 (en) | 2013-03-15 | 2016-05-24 | Epizyme, Inc. | CARM1 inhibitors and uses thereof |
| KR20160003647A (ko) | 2013-03-15 | 2016-01-11 | 에피자임, 인코포레이티드 | Carm1 억제제 및 이의 용도 |
| EP3038623A4 (en) * | 2013-09-09 | 2017-04-19 | Melinta Therapeutics, Inc. | Antimicrobial compounds and methods of making and using the same |
| AU2014315050A1 (en) * | 2013-09-09 | 2016-03-24 | Melinta Therapeutics, Inc. | Antimicrobial compunds and methods of making and using the same |
| US20180141897A1 (en) | 2014-12-08 | 2018-05-24 | The Research Foundation For The State University Of New York | Anti-fungals targeting the synthesis of fungal shingolipids |
| CA2979342A1 (en) * | 2015-03-11 | 2016-09-15 | Melinta Therapeutics, Inc. | Antimicrobial compounds and methods of making and using the same |
| CN105669519B (zh) * | 2016-01-04 | 2018-01-05 | 北方民族大学 | 吲哚类化合物、制备方法及其作为抗耐药菌药物的应用 |
| MX2018013545A (es) | 2016-05-06 | 2019-08-14 | Melinta Therapeutics Inc | Antimicrobianos y metodos de preparacion y uso de los mismos. |
| WO2017193016A1 (en) | 2016-05-06 | 2017-11-09 | Melinta Therapeutics, Inc. | Antimicrobials and methods of making and using same |
| WO2017193023A1 (en) * | 2016-05-06 | 2017-11-09 | Melinta Therapeutics, Inc. | Antimicrobials and methods of making and using same |
| EP3638649A4 (en) | 2017-06-16 | 2021-03-17 | The Research Foundation for The State University of New York | FUNGUSKID AGENTS AGAINST THE SYNTHESIS OF FUNGAL SHINGOLIPIDS |
| AU2018288665A1 (en) | 2017-06-19 | 2019-12-19 | Ashoke Bhattacharjee | Antimicrobials and methods of making and using same |
| WO2019164880A1 (en) * | 2018-02-21 | 2019-08-29 | Duffy Erin M | Antimicrobials and methods of making and using same |
| US20210253577A1 (en) | 2018-06-06 | 2021-08-19 | BioVersys AG | Biodefense agents |
| WO2019234509A2 (en) | 2018-06-06 | 2019-12-12 | BioVersys AG | Aminomethylamidine and methylamidine antimicrobial compounds |
| WO2020115547A2 (en) * | 2018-12-07 | 2020-06-11 | BioVersys AG | Pyrrolo[2,3-d]pyrimidin-2-one antimicrobial compounds |
| WO2021097061A1 (en) * | 2019-11-13 | 2021-05-20 | Curza Global, Llc | Antimicrobial compounds and methods |
| CN111254091B (zh) * | 2020-01-20 | 2022-04-19 | 浙江工业大学 | 一种嗜麦芽窄食单胞菌gyh及其在降解氯代烃类污染物中的应用 |
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| US4522811A (en) | 1982-07-08 | 1985-06-11 | Syntex (U.S.A.) Inc. | Serial injection of muramyldipeptides and liposomes enhances the anti-infective activity of muramyldipeptides |
| JP2873340B2 (ja) | 1988-04-29 | 1999-03-24 | 武田薬品工業株式会社 | 抗生物質ｔａｎ―１０５７，その製造法および用途 |
| US5958930A (en) | 1991-04-08 | 1999-09-28 | Duquesne University Of The Holy Ghost | Pyrrolo pyrimidine and furo pyrimidine derivatives |
| US5763263A (en) | 1995-11-27 | 1998-06-09 | Dehlinger; Peter J. | Method and apparatus for producing position addressable combinatorial libraries |
| GB9708611D0 (en) | 1997-04-28 | 1997-06-18 | Univ Cardiff | Chemical compounds |
| CA2297055A1 (en) | 1997-08-07 | 1999-02-18 | Research Corporation Technologies, Inc. | Antibiotic for methicillin resistant bacteria |
| DE19838998A1 (de) | 1998-08-27 | 2000-03-09 | Bayer Ag | Neue Naturstoffderivate |
| EP1113008A1 (en) | 1999-12-29 | 2001-07-04 | Pfizer Products Inc. | 4-oxo-2-ureido-1,4,5,6-tetrahydro-pyrimidine derivatives useful as antibacterial and antiprotozoal agents |
| KR100358083B1 (ko) * | 2000-02-17 | 2002-10-25 | 에스케이케미칼주식회사 | 피롤로피리미디논 유도체와 이의 제조방법, 그리고 이의용도 |
| DE10061538A1 (de) | 2000-12-11 | 2002-06-20 | Bayer Ag | Ureido-Dihydropyrimidinone |
| DE10061537A1 (de) | 2000-12-11 | 2002-06-20 | Bayer Ag | beta-Alanin-Derivate |
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| DE10061541A1 (de) | 2000-12-11 | 2002-06-20 | Bayer Ag | Arylamino-Dihydropyrimidinone |
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2012
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- 2012-04-11 JP JP2014505231A patent/JP6317669B2/ja active Active
- 2012-04-11 EA EA201391536A patent/EA201391536A1/ru unknown
- 2012-04-11 KR KR1020137030273A patent/KR20140065378A/ko not_active Application Discontinuation
- 2012-04-11 DK DK12799934.0T patent/DK2697229T3/en active
- 2012-04-11 HU HUE12799934A patent/HUE036755T2/hu unknown
- 2012-04-11 WO PCT/US2012/032994 patent/WO2012173689A2/en active Application Filing
- 2012-04-11 EP EP12799934.0A patent/EP2697229B1/en active Active
- 2012-04-11 SG SG10201603027QA patent/SG10201603027QA/en unknown
- 2012-04-11 CN CN201810630324.1A patent/CN109053695A/zh active Pending
- 2012-04-11 SG SG2013076575A patent/SG194489A1/en unknown
- 2012-04-11 EP EP18162332.3A patent/EP3404028A1/en not_active Withdrawn
- 2012-04-11 MY MYPI2013003732A patent/MY173518A/en unknown
- 2012-04-11 MX MX2013012015A patent/MX357903B/es active IP Right Grant
- 2012-04-11 AU AU2012271228A patent/AU2012271228B2/en not_active Ceased
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- 2012-04-11 CN CN201280029215.5A patent/CN103958514B/zh not_active Expired - Fee Related
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